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SV40大T抗原的细胞周期调控对T抗原表达水平的依赖性。

Dependence of SV40 large T-antigen cell cycle regulation on T-antigen expression levels.

作者信息

Sladek T L, Jacobberger J W

机构信息

Department of Genetics, Case Western Reserve University, School of Medicine, Cleveland, Ohio 44106.

出版信息

Oncogene. 1992 Jul;7(7):1305-13.

PMID:1620545
Abstract

Simian virus 40 (SV40) large T antigen (Tag) expression results in reduced percentages of G1-phase cells and increased percentages of S- and G2+M-phase cells in exponentially growing fibroblast populations as compared with identical cell populations not expressing Tag. This effect is the result of reduced G1 and increased G2+M cell cycle phase durations caused by Tag [Sladek, T.L. & Jacobberger, J.W. (1992). J. Virol., 66, 1059-1065]. Using recombinant retroviruses to manipulate Tag expression over a 25-fold range, it is shown here that the magnitude of this cell cycle phenotype increases as a function of increasing intracellular Tag concentration. This effect of Tag on the cell cycle is not independent of negative regulation by cellular mechanisms since exponentially growing cell populations producing high and increasing levels of Tag, increase the fraction of cells residing in G1 and decrease the fraction in S and G2+M as a function of cell density. Therefore, the data in this paper show, first, that Tag is a concentration-dependent, positive cell cycle regulator in exponentially proliferating cells and, second, that endogenous cellular mechanisms negatively regulating the cell cycle in response to cell density override the effect of Tag.

摘要

与不表达猿猴病毒40(SV40)大T抗原(Tag)的相同细胞群体相比,在指数生长的成纤维细胞群体中,SV40大T抗原(Tag)的表达导致G1期细胞百分比降低,S期和G2+M期细胞百分比增加。这种效应是由Tag导致的G1期缩短和G2+M期细胞周期持续时间延长的结果[Sladek, T.L. & Jacobberger, J.W. (1992). J. Virol., 66, 1059 - 1065]。利用重组逆转录病毒在25倍的范围内操纵Tag表达,本文表明这种细胞周期表型的程度随着细胞内Tag浓度的增加而增加。Tag对细胞周期的这种作用并非独立于细胞机制的负调控,因为随着细胞密度的增加,指数生长的细胞群体中产生高水平且不断增加的Tag,会使处于G1期的细胞比例增加,而处于S期和G2+M期的细胞比例减少。因此,本文的数据首先表明,在指数增殖的细胞中,Tag是一种浓度依赖性的正性细胞周期调节因子;其次表明,响应细胞密度负调控细胞周期的内源性细胞机制会抵消Tag的作用。

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